FDA 510(k)

D2P

K-Number: K161841 · 2017-01-09

Decision Date2017-01-09

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

D2P is the device name listed in this FDA 510(k) record. The listed applicant is 3D Systems, Inc.. It received FDA 510(k) clearance on 2017-01-09 under 510(k) number K161841. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the D2P?

D2P is a medical device that received FDA 510(k) clearance on 2017-01-09. The listed applicant is 3D Systems, Inc.. The 510(k) number is K161841.

When did D2P receive FDA 510(k) clearance?

D2P received FDA 510(k) clearance on 2017-01-09, under 510(k) number K161841.

Who is the listed applicant for D2P?

The FDA 510(k) record lists 3D Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for D2P?

The FDA product code for D2P is LLZ.

Other records listing 3D Systems, Inc. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.